Quality Assurance Engineer

Magenta Medical
Magenta Medical

Quality Assurance · Full-time

Magenta, Metropolitan City of Milan, Italy

Posted on Jul 8, 2026

Description

We are seeking an experienced Quality Assurance Engineer to join our QA Operations team and support a variety of activities related to QA Operations, such as:

  • Managing Supplier Quality Issues and coordinating cross-functional activities with Engineering, Purchasing, Manufacturing, and R&D to resolve supplier quality issues and minimize production impact.
  • Serve as the primary Quality representative for resolving nonconformances identified during Incoming Quality Control (IQC) inspections.
  • Review and assess incoming inspection failures to determine the appropriate disposition and escalation path, and to continuously improve incoming inspection processes.
  • Lead and perform the Engineering Change Order (ECO) process from risk analysis through protocol approval.
  • Verification, execution, and analysis of reposts until FDA-ready.
  • Provide guidance to the R&D and Engineering teams on IQ/OQ/PV activities.

Reports to

QA Manager

Requirements

  • B.A. or B.S. degree in a technical discipline, such as Engineering or Science.
  • 3-5 years of relevant experience in a Quality Engineering role in the medical device industry.
  • Previous experience with medical device Quality issues investigation, verification/validations, ECOs.
  • Strong understanding of Quality Management Systems (QMS) and applicable standards, including ISO 13485 and FDA 21 CFR Part 820 (or FDA QMSR).
  • Ability to work independently with minimal work direction and in a cross-functional team environment.
  • Fluent in English with excellent writing skills, effective written and verbal communication skills.
  • Excellent computer skills, including a working knowledge of Microsoft Office applications.
  • Strong time and project management abilities
  • Detail-oriented.